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Episodic ataxia type 2
MONDO:0007163A form of hereditary episodic ataxia (EA) characterized by paroxysmal episodes of ataxia lasting hours, with interictal nystagmus and mildly progressive ataxia.
Also known as: CACNA1A hereditary episodic ataxia, episodic ataxia type 2, hereditary episodic ataxia caused by mutation in CACNA1A, APCA, Acetazolamide-responsive episodic ataxia syndrome, Acetazolamide-responsive hereditary paroxysmal cerebellar ataxia, Acetazolamide-responsive, hereditary, paroxysmal, cerebellar ataxia, CAPA
3 clinical trials for this condition and its sub-types.
Follow this condition to get notified about new trialsBroader categories
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New keyboard designs aim to boost typing speed for people with movement challenges
Symptom relief CompletedThis study compares different visual keyboard layouts to see which helps people with complex sensorimotor disabilities type faster and with less fatigue. Twelve adults who already use a virtual scanning keyboard will test each layout. The goal is to find the best design to improv…
Sponsor: Assistance Publique - Hôpitaux de Paris • Aim: Symptom relief
Last updated Jul 18, 2026 00:00 UTC
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New parent support programme shows promise for families of children with complex needs
Symptom relief CompletedThis pilot study tested a community-based group programme called 'Encompass' for parents of children under 5 with complex neurodisability. Fifteen parents in East London attended ten group sessions over six months. The study aimed to see if the programme was feasible and acceptab…
Sponsor: City, University of London • Aim: Symptom relief
Last updated Jun 27, 2026 12:05 UTC